ปรัชญา: ความสำเร็จที่แท้จริงอยู่ที่การนำความรู้ไปประยุกต์ใช้เพื่อประโยชน์สุขแก่มวลมนุษยชาติ

You are here

ผลงานวิจัย

2021

 

1. Splint Padding Thickness: Temperature Effects and X-ray Visualization. Everson PJ, Sura T, Udawatta T, Nicolaou D, Watson JT. J Orthop Trauma. 2021 Sep 1;35(9):e341-e345. doi: 10.1097/BOT.0000000000002051. PMID: 33512858

2. Amelioration of osteogenesis in iPSC-derived mesenchymal stem cells from osteogenesis imperfecta patients by endoplasmic reticulum stress inhibitor. Duangchan T, Tawonsawatruk T, Angsanuntsukh C, Trachoo O, Hongeng S, Kitiyanant N, Supokawej A. Life Sci. 2021 Aug 1;278:119628. doi: 10.1016/j.lfs.2021.119628. Epub 2021 May 18. PMID: 34015290

3. Surviving serum - the E. coli iss gene (increased serum survival) of extraintestinal pathogenic E. coli (ExPEC) is required for the synthesis of group 4 cpsule. Biran D, Sura T, Otto A, Yair Y, Becher D, Ron EZ. Infect Immun. 2021 Jun 28:IAI0031621. doi: 10.1128/IAI.00316-21. Online ahead of print. PMID: 34181459

4. Proteomic Adaptation of Clostridioides difficile to Treatment with the Antimicrobial Peptide Nisin. Maaß S, Bartel J, Mücke PA, Schlüter R, Sura T, Zaschke-Kriesche J, Smits SHJ, Becher D. Cells. 2021 Feb 11;10(2):372. doi: 10.3390/cells10020372. PMID: 33670309.

5. Cost-minimization analysis of sequential genetic testing versus targeted next-generation sequencig gene panels in patients with pheochromocytoma and paraganglioma. Pipitprapat W, Pattanaprateep O, Iemwimangsa N, Sensorn I, Panthan B, Jiaranai P, Chantratita W, Sorapipatcharoen K, Poomthavorn P, Mahachoklertwattana P, Sura T, Tunteeratum A, Srichan K, Sriphrapradang C. Ann Med. 2021 Dec;53(1):1243-1255. doi: 10.1080/07853890.2021.1956687. PMID: 34309460.

6. Changing expression patterns of TonB-dependent transporters suggest shifts in polysaccharide consumption over the course of a spring phytoplankton bloom. Francis TB, Bartosik D, Sura T, Sichert A, Hehemann JH, Markert S, Schweder T, Fuchs BM, Teeling H, Amann RI, Becher D. ISME J. 2021 Aug;15(8):2336-2350. doi: 10.1038/s41396-021-00928-8. Epub 2021 Mar 1. PMID: 33649555.

7. Kidney Autotransplantation for Treatment of Ureteric Obstruction: A Case Report and Brief Review of the Literature.Joshi P, Lin J, Sura T, Limbu PS, Melkonian V, Bastani B, Varma C. Case Rep Surg. 2021 Jul 21;2021:6646958. doi: 10.1155/2021/6646958. eCollection 2021. PMID: 34336349.

8. Treatment of Hepatitis C Post-Liver Transplantation Could Mitigate Discard Rates of Hepatitis C-Positive Deceased Donor Livers and Expand the Donor Pool. Keller J, Marklin G, Okoye O, Desai R, Sura T, Jain A, Varma C, Nazzal M. J Transplant. 2021 Jan 25;2021:6612453. doi: 10.1155/2021/6612453. eCollection 2021. PMID: 33564467.

9. Operative management of an incidental portal vein aneurysm in the setting of an incarcerated congenital diaphragmatic hernia. Sura TA, Boutrous ML, Ruiz MI, Williams MS. J Vasc Surg Cases Innov Tech. 2020 Oct 27;7(1):64-67. doi: 10.1016/j.jvscit.2020.10.009. eCollection 2021 Mar.

 

2020

1. Optimized Proteomics Workflow for the Detection of Small Proteins. Bartel J, Varadarajan AR, Sura T, Ahrens CH, Maaß S, Becher D. J Proteome Res. 2020 Oct 2;19(10):4004-4018. doi: 10.1021/acs.jproteome.0c00286. Epub 2020 Sep 2. PMID: 32812434

2. Interplay between vitamin D receptor FokI polymorphism and smoking influences Porphyromonas gingivalis proportions in subgingival plaque. Torrungruang K, Chantarangsu S, Sura T, Thienpramuk L. J Clin Periodontol. 2020 Aug;47(8):912-920. doi: 10.1111/jcpe.13307. Epub 2020 Jun 3. PMID: 32418218

3. Membrane Modulation of Super-Secreting "midiBacillus" Expressing the Major Staphylococcus aureus Antigen - A Mass-Spectrometry-Based Absolute Quantification Approach. Antelo-Varela M, Aguilar Suárez R, Bartel J, Bernal-Cabas M, Stobernack T, Sura T, van Dijl JM, Maaß S, Becher D. Front Bioeng Biotechnol. 2020 Feb 28;8:143. doi: 10.3389/fbioe.2020.00143. eCollection 2020. PMID: 32185169.

4. TRIM29 is required for efficient recruitment of 53BP1 in response to DNA double-strand breaks in vertebrate cells. Wikiniyadhanee R, Lerksuthirat T, Stitchantrakul W, Chitphuk S, Sura T, Dejsuphong D. FEBS Open Bio. 2020 Oct;10(10):2055-2071. doi: 10.1002/2211-5463.12954. Epub 2020 Aug 31. PMID: 33017104.

5. Operative management of an incidental portal vein aneurysm in the setting of an incarcerated congenital diaphragmatic hernia. Sura TA, Boutrous ML, Ruiz MI, Williams MS. J Vasc Surg Cases Innov Tech. 2020 Oct 27;7(1):64-67. doi: 10.1016/j.jvscit.2020.10.009. eCollection 2021 Mar. PMID: 33665534.

 

2019

 

  1. Training in clinical genetics and genetic counseling in Asia. Cutiongco-de la Paz EM, Chung BH, Faradz SMH, Thong MK, David-Padilla C, Lai PS, Lin SP, Chen YH, Sura T, Laurino M. Am J Med Genet C Semin Med Genet. 2019 Jun;181(2):177-186. doi: 10.1002/ajmg.c.31703. Epub 2019 Apr 29. PMID: 31037827 Review.

  2. The lateral preoptic area and ventral pallidum embolden behavior. Reichard RA, Parsley KP, Subramanian S, Stevenson HS, Schwartz ZM, Sura T, Zahm DS. Brain Struct Funct. 2019 Apr;224(3):1245-1265. doi: 10.1007/s00429-018-01826-0. Epub 2019 Jan 24. PMID: 30680454.

  3. Factors associated with dependence on smokeless tobacco, Navi Mumbai, India. Salvi A, Sura T, Karaye I, Horney JA. Heliyon. 2019 Mar 19;5(3):e01382. doi: 10.1016/j.heliyon.2019.e01382. eCollection 2019 Mar. PMID: 30949610.

  4. Carrier frequency of spinal muscular atrophy in Thailand. Dejsuphong D, Taweewongsounton A, Khemthong P, Chitphuk S, Stitchantrakul W, Sritara P, Tunteeratum A, Sura T. Neurol Sci. 2019 Aug;40(8):1729-1732. doi: 10.1007/s10072-019-03885-5. Epub 2019 Apr 19. PMID: 31004230

  5. Oral manifestations in patients and dogs with mucopolysaccharidosis Type VII. Kantaputra PN, Smith LJ, Casal ML, Kuptanon C, Chang YC, Nampoothiri S, Paiyarom A, Veerasakulwong T, Trachoo O, Ketudat Cairns JR, Chinadet W, Tanpaiboon P. Am J Med Genet A. 2019 Mar;179(3):486-493. doi: 10.1002/ajmg.a.61034. Epub 2019 Jan 17. PMID: 30653816.

  6. Clinical utility of combined preimplantation genetic testing methods in couples at risk of passing on beta thalassemia/hemoglobin E disease: A retrospective review from a single center. Satirapod C, Sukprasert M, Panthan B, Charoenyingwattana A, Chitayanan P, Chantratita W, Choktanasiri W, Trachoo O, Hongeng S. PLoS One. 2019 Nov 21;14(11):e0225457. doi: 10.1371/journal.pone.0225457. eCollection 2019. PMID: 31751397.

  7. Far-reaching cellular consequences of tat deletion in Escherichia coli revealed by comprehensive proteome analyses. Dolata KM, Montero IG, Miller W, Sievers S, Sura T, Wolff C, Schlüter R, Riedel K, Robinson C. Microbiol Res. 2019 Jan;218:97-107. doi: 10.1016/j.micres.2018.10.008. Epub 2018 Nov 1. PMID: 30454663 Free article.

  8. Comparative proteome analysis in an Escherichia coli CyDisCo strain identifies stress responses related to protein production, oxidative stress and accumulation of misfolded protein. Guerrero Montero I, Dolata KM, Schlüter R, Malherbe G, Sievers S, Zühlke D, Sura T, Dave E, Riedel K, Robinson C. Microb Cell Fact. 2019 Jan 29;18(1):19. doi: 10.1186/s12934-019-1071-7. PMID: 30696436.

  9. Novel PANK2 mutation discovered among South East Asian children living in Thailand affected with pantothenate kinase associated neurodegeneration. Sakpichaisakul K, Saengow VE, Suwanpratheep P, Rongnoparat K, Panthan B, Trachoo O. J Clin Neurosci. 2019 Aug;66:187-190. doi: 10.1016/j.jocn.2019.04.017. Epub 2019 May 11. PMID: 31088771

  10. Ariadne's Thread in the Analytical Labyrinth of Membrane Proteins: Integration of Targeted and Shotgun Proteomics for Global Absolute Quantification of Membrane Proteins. Antelo-Varela M, Bartel J, Quesada-Ganuza A, Appel K, Bernal-Cabas M, Sura T, Otto A, Rasmussen M, van Dijl JM, Nielsen A, Maaß S, Becher D. Anal Chem. 2019 Sep 17;91(18):11972-11980. doi: 10.1021/acs.analchem.9b02869. Epub 2019 Sep 3.

 

2018

 

  1. Proteomic response of Streptococcus pneumoniae to iron limitation. Hoyer J, Bartel J, Gómez-Mejia A, Rohde M, Hirschfeld C, Heß N, Sura T, Maaß S, Hammerschmidt S, Becher D. Int J Med Microbiol. 2018 Aug;308(6):713-721. doi: 10.1016/j.ijmm.2018.02.001. Epub 2018 Feb 13. PMID: 29496408

  2. The Escherichia coli Type III Secretion System 2 Has a Global Effect on Cell Surface. Shulman A, Yair Y, Biran D, Sura T, Otto A, Gophna U, Becher D, Hecker M, Ron EZ. mBio. 2018 Jul 3;9(4):e01070-18. doi: 10.1128/mBio.01070-18. PMID: 29970469.

  3. Far-reaching cellular consequences of tat deletion in Escherichia coli revealed by comprehensive proteome analyses. Dolata KM, Montero IG, Miller W, Sievers S, Sura T, Wolff C, Schlüter R, Riedel K, Robinson C. Microbiol Res. 2019 Jan;218:97-107. doi: 10.1016/j.micres.2018.10.008. Epub 2018 Nov 1. PMID: 30454663 Free article.

  4. A Secreted Bacterial Peptidylarginine Deiminase Can Neutralize Human Innate Immune Defenses. Stobernack T, du Teil Espina M, Mulder LM, Palma Medina LM, Piebenga DR, Gabarrini G, Zhao X, Janssen KMJ, Hulzebos J, Brouwer E, Sura T, Becher D, van Winkelhoff AJ, Götz F, Otto A, Westra J, van Dijl JM. mBio. 2018 Oct 30;9(5):e01704-18. doi: 10.1128/mBio.01704-18. PMID: 30377277.

  5. A Report on Ten Asia Pacific Countries on Current Status and Future Directions of the Genetic Counseling Profession: The Establishment of the Professional Society of Genetic Counselors in Asia. Laurino MY, Leppig KA, Abad PJ, Cham B, Chu YWY, Kejriwal S, Lee JMH, Sternen DL, Thompson JK, Burgess MJ, Chien S, Elackatt N, Lim JY, Sura T, Faradz S, Padilla C, Paz ECD, Nauphar D, Nguyen KN, Zayts O, Vu DC, Thong MK. J Genet Couns. 2018 Feb;27(1):21-32. doi: 10.1007/s10897-017-0115-6. Epub 2017 Jul 11.

 

2017

 

  1. First successful trial of preimplantation genetic diagnosis for pantothenate kinase-associated neurodegeneration.

  2. Trachoo O, Satirapod C, Panthan B, Sukprasert M, Charoenyingwattana A, Chantratita W, Choktanasiri W, Hongeng S. J Assist Reprod Genet. 2017 Jan;34(1):109-116. doi: 10.1007/s10815-016-0833-y. Epub 2016 Nov 4. PMID: 27815806.

  3. A Report on Ten Asia Pacific Countries on Current Status and Future Directions of the Genetic Counseling Profession: The Establishment of the Professional Society of Genetic Counselors in Asia. Laurino MY, Leppig KA, Abad PJ, Cham B, Chu YWY, Kejriwal S, Lee JMH, Sternen DL, Thompson JK, Burgess MJ, Chien S, Elackatt N, Lim JY, Sura T, Faradz S, Padilla C, Paz ECD, Nauphar D, Nguyen KN, Zayts O, Vu DC, Thong MK. J Genet Couns. 2018 Feb;27(1):21-32. doi: 10.1007/s10897-017-0115-6. Epub 2017 Jul 11. PMID: 28699126

  4. Genotype-Phenotype Correlation in Patients With Germline Mutations of VHL, RET, SDHB, and SDHD Genes: Thai Experience. Sriphrapradang C, Choopun K, Tunteeratum A, Sura T. Clin Med Insights Endocrinol Diabetes. 2017 Apr 20;10:1179551417705122. doi: 10.1177/1179551417705122. eCollection 2017. PMID: 28469506.

  5. Exome sequencing for simultaneous mutation screening in children with hemophagocytic lymphohistiocytosis. Mukda E, Trachoo O, Pasomsub E, Tiyasirichokchai R, Iemwimangsa N, Sosothikul D, Chantratita W, Pakakasama S. Int J Hematol. 2017 Aug;106(2):282-290. doi: 10.1007/s12185-017-2223-3. Epub 2017 Mar 28. PMID: 28353193

  6. A Novel PRKAR1A Mutation Identified in a Patient with Isolated Primary Pigmented Nodular Adrenocortical Disease. Korpaisarn S, Trachoo O, Panthan B, Aroonroch R, Suvikapakornkul R, Sriphrapradang C. Case Rep Oncol. 2017 Aug 16;10(2):769-776. doi: 10.1159/000479585. eCollection 2017 May-Aug. PMID: 28878664.

  7. Low oxygen saturation and severe anemia in compound heterozygous Hb Louisville [β42(CD1)Phe→Leu] and Hb La Desirade [β129(H7)Ala→Val]. Kamseng P, Trakulsrichai S, Trachoo O, Yimniam W, Panthan B, Jittorntam P, Niparuck P, Sanguanwit P, Wananukul W, Jindadamrongwech S. Hematology. 2017 Mar;22(2):114-118. doi: 10.1080/10245332.2016.1231989. Epub 2016 Sep 27. PMID: 27670359

  8. Abundant collateralization of temporal lobe projections to the accumbens, bed nucleus of stria terminalis, central amygdala and lateral septum. Reichard RA, Subramanian S, Desta MT, Sura T, Becker ML, Ghobadi CW, Parsley KP, Zahm DS. Brain Struct Funct. 2017 May;222(4):1971-1988. doi: 10.1007/s00429-016-1321-y. Epub 2016 Oct 4. PMID: 27704219.

  9. Clinical course over five decades of a woman carrying 16p13.3 microduplication. Pibalyart S, Trachoo O. Clin Dysmorphol. 2017 Oct;26(4):217-220. doi: 10.1097/MCD.0000000000000189.

 

2016

  1. Proteomics of septicemic Escherichia coli. Otto A, Biran D, Sura T, Becher D, Ron EZ. Proteomics Clin Appl. 2016 Oct;10(9-10):1020-1024. doi: 10.1002/prca.201600049. PMID: 27604157 Review.

  2. First successful trial of preimplantation genetic diagnosis for pantothenate kinase-associated neurodegeneration. Trachoo O, Satirapod C, Panthan B, Sukprasert M, Charoenyingwattana A, Chantratita W, Choktanasiri W, Hongeng S. J Assist Reprod Genet. 2017 Jan;34(1):109-116. doi: 10.1007/s10815-016-0833-y. Epub 2016 Nov 4. PMID: 27815806.

  3. Angiotensin-converting enzyme gene polymorphism in Thai patients with systemic lupus erythematosus. Pitipakorn U, Suwannalai P, Trachoo O, Rattanasiri S, Chitphuk S, Ngamjanyaporn P, Sura T. Int J Rheum Dis. 2016 Jul;19(7):693-9. doi: 10.1111/1756-185X.12609. Epub 2015 Jul 22. PMID: 26200015

  4. Screening of Fabry disease in patients with end-stage renal disease of unknown etiology: the first Thailand study. Trachoo O, Jittorntam P, Pibalyart S, Kajanachumphol S, Suvachittanont N, Patputthipong S, Chuengsaman P, Nongnuch A. J Biomed Res. 2016 Oct 17;31(1):17-24. doi: 10.7555/JBR.31.20160063. PMID: 28808181.

  5. A Novel Mutation in Thyroid Peroxidase Gene Causing Congenital Goitrous Hypothyroidism in a German-Thai Patient. Sriphrapradang C, Thewjitcharoen Y, Chanprasertyothin S, Nakasatien S, Himathongkam T, Trachoo O. J Clin Res Pediatr Endocrinol. 2016 Jun 5;8(2):241-5. doi: 10.4274/jcrpe.2503. Epub 2015 Jan 18. PMID: 26761947.

  6. Vitamin D Receptor Gene Polymorphism and Smoking in the Risk of Chronic Periodontitis. Chantarangsu S, Sura T, Mongkornkarn S, Donsakul K, Torrungruang K. J Periodontol. 2016 Nov;87(11):1343-1351. doi: 10.1902/jop.2016.160222. Epub 2016 Aug 4. PMID: 27491013

  7. FIRST IDENTIFICATION OF HEMOGLOBIN LANSINGRAMATHIBODI [α87(F8)His → Gln; CAC>CAG (HBA1: c.264C>G)] IN A THAI FAMILY WITH SPURIOUS HYPOXEMIA. Trakulsrichai S, Panthan B, Jittorntam P, Niparuck P, Sriapha C, Chantratita W, Wananukul W, Trachoo O. Southeast Asian J Trop Med Public Health. 2016 Sep;47(5):1048-54. PMID: 29620819

  8. Low oxygen saturation and severe anemia in compound heterozygous Hb Louisville [β42(CD1)Phe→Leu] and Hb La Desirade [β129(H7)Ala→Val]. Kamseng P, Trakulsrichai S, Trachoo O, Yimniam W, Panthan B, Jittorntam P, Niparuck P, Sanguanwit P, Wananukul W, Jindadamrongwech S. Hematology. 2017 Mar;22(2):114-118. doi: 10.1080/10245332.2016.1231989. Epub 2016 Sep 27. PMID: 27670359

  9. Abundant collateralization of temporal lobe projections to the accumbens, bed nucleus of stria terminalis, central amygdala and lateral septum. Reichard RA, Subramanian S, Desta MT, Sura T, Becker ML, Ghobadi CW, Parsley KP, Zahm DS. Brain Struct Funct. 2017 May;222(4):1971-1988. doi: 10.1007/s00429-016-1321-y. Epub 2016 Oct 4.

 

2015

 

  1. Angiotensin-converting enzyme gene polymorphism in Thai patients with systemic lupus erythematosus. Pitipakorn U, Suwannalai P, Trachoo O, Rattanasiri S, Chitphuk S, Ngamjanyaporn P, Sura T. Int J Rheum Dis. 2016 Jul;19(7):693-9. doi: 10.1111/1756-185X.12609. Epub 2015 Jul 22. PMID: 26200015

  2. A Novel Mutation in Thyroid Peroxidase Gene Causing Congenital Goitrous Hypothyroidism in a German-Thai Patient. Sriphrapradang C, Thewjitcharoen Y, Chanprasertyothin S, Nakasatien S, Himathongkam T, Trachoo O. J Clin Res Pediatr Endocrinol. 2016 Jun 5;8(2):241-5. doi: 10.4274/jcrpe.2503. Epub 2015 Jan 18. PMID: 26761947.

  3. Environmental lead exposure, catalase gene, and markers of antioxidant and oxidative stress relation to hypertension: an analysis based on the EGAT study. Sirivarasai J, Kaojarern S, Chanprasertyothin S, Panpunuan P, Petchpoung K, Tatsaneeyapant A, Yoovathaworn K, Sura T, Kaojarern S, Sritara P. Biomed Res Int. 2015;2015:856319. doi: 10.1155/2015/856319. Epub 2015 Feb 22.

 

2014

  1. Fine-needle aspiration cytology of parathyroid carcinoma mimic hürthle cell thyroid neoplasm. Chutintorn Sriphrapradang , Pattana Sornmayura , Niramol Chanplakorn , Trachoo Objoon , Pattarana Sae-Chew , Rangsima Aroonroch
    Case Rep Endocrinol. 2014;2014:680876. doi: 10.1155/2014/680876. Epub 2014 Aug 10.

 

2013

 

  1. Association between inflammatory marker, environmental lead exposure, and glutathione S-transferase gene. Sirivarasai J, Wananukul W, Kaojarern S, Chanprasertyothin S, Thongmung N, Ratanachaiwong W, Sura T, Sritara P. Biomed Res Int. 2013;2013:474963. doi: 10.1155/2013/474963. Epub 2013 Jan 17. PMID: 23484121. Clinical Trial.

  2. Chromosome 22q11.2 deletion syndrome presenting as adult onset hypoparathyroidism: clues to diagnosis from dysmorphic facial features.Korpaisarn S, Trachoo O, Sriphrapradang C. Case Rep Endocrinol. 2013;2013:802793. doi: 10.1155/2013/802793. Epub 2013 Apr 30. PMID: 23738156.

  3. Chromosome 20p inverted duplication deletion identified in a Thai female adult with mental retardation, obesity, chronic kidney disease and characteristic facial features. Trachoo O, Assanatham M, Jinawath N, Nongnuch A. Eur J Med Genet. 2013 Jun;56(6):319-24. doi: 10.1016/j.ejmg.2013.03.011. Epub 2013 Mar 29.

 

2012

1. Genetic variations of glutathione s-transferase influence on blood cadmium concentration. Khansakorn N, Wongwit W, Tharnpoophasiam P, Hengprasith B, Suwannathon L, Chanprasertyothin S, Sura T, Kaojarern S, Sritara P, Sirivarasai J. J Toxicol. 2012;356126.

 

2011

 

1. A genetic association study between growth differentiation factor 5 (GDF 5) polymorphism and knee osteoarthritis in Thai population. Tawonsawatruk T, Changthong T, Pingsuthiwong S, Trachoo O, Sura T, Wajanavisit W. J Orthop Surg Res. 2011 Sep 21;6:47. doi: 10.1186/1749-799X-6-47. PMID: 21936909.

2. Genome-wide association study identifies variations in 6p21.3 associated with nevirapine-induced rash. Chantarangsu S, Mushiroda T, Mahasirimongkol S, Kiertiburanakul S, Sungkanuparph S, Manosuthi W, Tantisiriwat W, Charoenyingwattana A, Sura T, Takahashi A, Kubo M, Kamatani N, Chantratita W, Nakamura Y. Clin Infect Dis. 2011 Aug;53(4):341-8. doi: 10.1093/cid/cir403. PMID: 21810746

3. The influence of metabolic gene polymorphisms on urinary 1-hydroxypyrene concentration in Thai bus drivers. Petchpoung K, Kaojarern S, Yoovathaworn K, Sura T, Sirivarasai J. Environ Toxicol Pharmacol. 2011 Jan;31(1):160-4. doi: 10.1016/j.etap.2010.10.006. Epub 2010 Oct 23. PMID: 21787681

4. Analysis of exon 8 of ATP7B gene in Thai patients with Wilson disease. Keandaungjuntr J, Busabaratana M, Kositchaiwat C, Sura T, Pulkes T. J Med Assoc Thai. 2011 Oct;94(10):1184-8. PMID: 22145502

5. Biochemical, environmental, and genetic factors associated with paraoxonase (PON1) activity. Sirivarasai J, Kaojarern S, Sura T, Yoovathaworn K. Biochem Genet. 2011 Jun;49(5-6):364-8. doi: 10.1007/s10528-010-9413-5. Epub 2011 Jan 22.

 

 

 

  1. Eu-ahsunthornwattana J, Trachoo O, Dejsuphong D, Tunteeratum A, Srichan K, Sura T. Noonan syndrome, metabolic syndrome and stroke-in-the-young: coincidence, causal or contribution? J Med Assoc Thai. 2010;93(9):1084-7.
  2. Phasukkijwatana N, Kunhapan B, Stankovich J, Chuenkongkaew WL, Thomson R, Thornton T, Bahlo M, Mushiroda T, Nakamura Y, Mahasirimongkol S, Tun AW, Srisawat C, Limwongse C, Peerapittayamongkol C, Sura T, Suthammarak W, Lertrit P. Genome-wide linkage scan and association study of PARL to the expression of LHON families in Thailand. Hum Genet. 2010;128(1):39-49.
  3. Lawaly YR, Sakuntabhai A, Marrama L, Konate L, Phimpraphi W, Sokhna C, Tall A, Sarr FD, Peerapittayamongkol C, Louicharoen C, Schneider BS, Levescot A, Talman A, Casademont I, Menard D, Trape JF, Rogier C, Kaewkunwal J, Sura T, Nuchprayoon I, Ariey F, Baril L, Singhasivanon P, Mercereau-Puijalon O, Paul R. Heritability of the human infectious reservoir of malaria parasites. PLoS One. 2010;29:5(6)
  4. Tawonsawatruk T, Trachoo O, Channom T, Sura T, Eu-ahsunthornwattana J, Woratanarat P, Wajanavisit W. Association of estrogen receptor-alpha single-nucleotide polymorphism (codon 594 G-->A) and Thai patients affected by knee osteoarthritis. J Med Assoc Thai. 2009;92 Suppl 6:S45-50.
  5. Louicharoen C, Patin E, Paul R, Nuchprayoon I, Witoonpanich B, Peerapittayamongkol C, Casademont I, Sura T, Laird NM, Singhasivanon P, Quintana-Murci L, Sakuntabhai A. Positively selected G6PD-Mahidol mutation reduces Plasmodium vivax density in Southeast Asians. Science. 2009;11;326(5959):1546-9.
  6. Tunteeratum A, Witoonpanich R, Phudhichareonrat S, Eu-ahsunthornwattana J, Pingsuthiwong S, Srichan K, Sura T. Congestive heart failure with rhabdomyolysis and acute renal failure in a manifesting female carrier of Duchenne muscular dystrophy with duplication of dystrophin gene. J Clin Neuromuscul Dis. 2009;11(1):49-53.
  7. Kamatani Y, Wattanapokayakit S, Ochi H, Kawaguchi T, Takahashi A, Hosono N, Kubo Tsunoda T, Kamatani N, Kumada H, Puseenam A, Sura T, Daigo Y, Chayama K, Chantratita W, Nakamura Y, Matsuda K. A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians. Nat Genet. 2009;41(5):591-5..
  8. Sura T, Eu-Ahsunthornwattana J, Youngcharoen S, Busabaratana M, Dejsuphong D, Trachoo O, Theerasasawat S, Tunteeratum A, Noparutchanodom C, Tunlayadechanont S. Frequencies of spinocerebellar ataxia subtypes in Thailand: window to the population history? J Hum Genet. 2009;54(5):284-8.
  9. Chantarangsu S, Mushiroda T, Mahasirimongkol S, Kiertiburanakul S, Sungkanuparph S, Manosuthi W, Tantisiriwat W, Charoenyingwattana A, Sura T, Chantratita W, Nakamura Y. HLA-B*3505 allele is a strong predictor for nevirapine-induced skin adverse drug reactions In HIV-infected Thai patients. Pharmacogenet Genomics. 2009;19(2):139-46.
  10. Mahasirimongkol S, Yanai H, Nishida N, Ridruechai C, Matsushita I, Ohashi J, Summanapan S, Yamada N, Moolphate S, Chuchotaworn C, Chaiprasert A, Manosuthi W, Kantipong P, Kanitwittaya S, Sura T, Khusmith S, Tokunaga K, Sawanpanyalert P, Keicho N. Genome-wide SNP-based linkage analysis of tuberculosis in Thais. Genes Immun. 2009;10(1):77-83.
  11. Phimpraphi W, Paul R, Witoonpanich B, Turbpaiboon C, Peerapittayamongkol C, Louicharoen C, Casademont I, Tungpradabkul S, Krudsood S, Kaewkunwal J, Sura T, Looareesuwan S, Singhasivanon P, Sakuntabhai A. Heritability of P. falciparum and P. vivax malaria in a Karen population in Thailand. PLoS One. 2008;3(12):e3887.
  12. Sura T, Eu-ahsunthornwattana J, Pingsuthiwong S, Busabaratana M. Sensitivity and frequencies of dystrophin gene mutations in Thai DMD/BMD patients as detected by multiplex PCR. Dis Markers. 2008;25(2):115-21.
  13. Kanechorn Na Ayuthya R, Patthamapasphong N, Sura T, Niumpradit N, Thachoo O. Ehlers-Danlos syndrome syndrome type IV with gastric adenocarcinoma. J Med Assoc Thai. 2008;91 Suppl 1:S166-71.
  14. Kiertiburanakul S, Sungkanuparph S, Charoenyingwattana A, Mahasirimongkol S, Sura T, Chantratia W. Risk factors for nevirapine-associated rash among HIV-infected patiens with low CD4 cell counts in resource-limited settings. Curr HIV Res. 2008;6(1):65-9
  15. Tocharoentanaphol C, Promso S, Zelenika D, Lowhnoo T, Tongsima S, Sura T, Chantratita W, Mastsuda F, Mooney S, Sakuntabhai A. Evaluation of resequencing on number of tag SNPs of 13 atherosclerosis-related genes in Thai population. J Hum Genet. 2008;53(1):74-86.
  16. Hongeng S, Pakakasama S, Chuansumrit A, Sirachainan N, Sura T, Ungkanont A, Chuncharunee S, Jootar S, Issaragisil S. Reduced intensity stem cell transplantation for treatment of calss 3 Lucarelli severe thalassemia patients. Am J Hematol. 2007;82(12):1095-8.
  17. Sura T, Busabaratana M, Youngcharoen S, Wisedpanichkij R, Viprakasit V, Trachoo O. Haemoglobin Hope in a northern Thai family:first identification of homozygous haemoglobin Hope associated with haemoglobin H disease. Eur J Haematol. 2007;79(3):251-4.
  18. Tantrittisak T, Sura T, Moleerergpoom W, Hanchaipiboolkul S. Plasma homocysteine and ischemic stroke patients in Thailand. J Med Assoc Thai. 2007;90(6):1183-7.
  19. Sirivarasai J, Kaojarern S, Yoovathaworn K, Sura T. Paraoxnase (PON1) polymorphism and activity as the determinants of sensitity to organopsphates in human subjects. Chem Biol Interact. 2007;20;168(3):184-92.
  20. Sura T, Trachoo O, Viprakasit V, Vathesatogkit p, Tunteeratum A, Busabaratana M, Wisedpanichkij R, Isarangkura P. Hemoglobin H disesse induced by the common SEA deletion and the rare hemoglobin Quong Sze in a Thai female: longitudinal clinical course, molecular characterization, and development of a PCR/RFLP-based detection methos. Ann hematol. 2007 May 15;
  21. Vasilescu A, Terashima Y, Enomoto M, Heath S, Poonpiriya V, Gatanaga H, Do H, Diop G, Hirtzig T, Auewarakul P, Lauhakirti D, Sura T, Charneau P, Marullo S, Therwath A, Oka S, Kanegasaki S, lathrop M, Matsushima K, Zagury JF, Matsuda F. A haplotype of the human CXCR1 gene protective against rapid disease progression in HIV-1+ patients. Proc Natl Acad Sci USA. 2007;27;104(9):3354-9.
  22. Wananukul W, Sura T. Salaitanawatwong P. Polymorphism of delta-aminolevulinic acid dehydratase and its effect on blood lead levels in Thai workers. Arch Environ Occup Health. 2006;61(2):67-72.
  23. Tharaphan P, Chuenkongkaew WL, Luangtrakool K, Sanpachudayan T, Suktitipat B, Suphavilai R, Srisawat C, Sura T, Lertrit P. Mitochondrial DNA haplogroup distribution in Pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy. J Neuroophthalmol. 2006;26(4):264-7.
  24. Mahasirimongkol S, Chantratita W, Promso S, Pasomsab E, Jinawath N, Jongjaroenprasert W, Lulitanond V, Krittayapoositpot P, Tongsima S, Sawanpanyalert P, Kamatani N, Nakamura Y, Sura T. Similarity of the allele frequency and linkage disequilibrium pattern of single nucleotide Polymorphisms in drug-related gene loci between Thai and northern East Asian populations: implications for tagging SNP selection in Thais. J Hum Genet. 2006;51(10):896-904.
  25. Phasukkijwatana N, Chuenkongkaew WL, Suphavilai R, Suktitipat B, Pingsuthiwong S, Ruangvaravate N, Atchaneeyasakul LO, Warrasak S, Poonyathalang A, Sura T, Lertrit P. The unique characteristics of Thai Leber hereditary optic neuropathy: analysis of 30 G11778A pedigrees. J Hum Genet. 2006;51(4):298-304.
  26. Witoonpanich R, Phankhian S, Sura T, Lertrit P, Phudhichareonrat S. Oculopharyngodistal myopathy in a Thai family. J Med Assoc Thai. 2004;87(12):1518-21.
  27. Moleerergpoom W, Sura T, Sritara P. Association between serum homocysteine, folate and B12 concentration with coronary artery disease in Thai patients. J Med Assoc Thai. 2004;87(6):674-8.
  28. Trachoo O, Sura T, Sakuntabhai A, Singhasivanon P, Krudsood S, Phimpraphi W, Krasaesub S, Chanjarunee S, Looareesuwan S. Molecular characterization of hereditary persistence of Fetal hemoglobin in the Karen people of Thailand. Hemoglobin. 2003;27(2):97-104.
  29. Sritara P, Cheepudomwit S, Chapman N, Woodward M, Kositchaiwat C, Tunlayadechanont S, Sura T, Hengprasith B, Tanphaichitr V, Lochaya S, Neal B, Tanomsup S, Yipintsoi T. Electricity Generating Authority of Thailand. Twelve-year changes in vascular risk factors And their associations with mortality in a cohort of 3499 Thais: the Electricity Generating Authority of Thailand Study. Int J 2003;32(3):461-8.
  30. Jones PG, Sura T, Harris M, Strother A. Mupirocin resistance in clinical isolates of Staphylococcus aureus. Infect Control Hosp Epidemiol. 2003;24(4):300-1.
  31. Limprasert P, Saechan V, Ruangdaraganon N, Sura T, Vasiknanote P, Jaruratanasirikul S, Brown WT. Haplotype analysis at the FRAXA locus in Thai subjects.Am J Med Genet. 2001;22;98(3):224-9.
  32. Limprasert P, Ruangdaraganon N, Vasiknanonte P, Sura T, Jaruratanasirikul S, Sriwongpanich N, Sriplung H. A clinical checklist for fragile X syndrome: screening of Thai boys With developmental delay of unknown cause. J Med Assoc Thai. 2000;83(10):1260-6.
  33. Angchaisuksiri P, Pingsuthiwong S, Sura T, Aryuchai K, Busabaratana M, Atichartakarn V. Prevalence of the C677T methylenetetra- hydrofolate reductase mutation in Thai patients with deep vein thrombosis.Acta Haematol. 2000;103(4):191-6.
  34. Angchaisuksiri P, Pingsuthiwong S, Aryuchai K, Busabaratana M, Sura T, Atichartakarn V, Sritara P. Prevalence of the G1691A mutation in the factor V gene (factor V Leiden) and the G20210A prothrombin gene mutation in the Thai population.Am J Hematol. 2000;65(2):119-22.
  35. Ruangdaraganon N, Limprasert P, Sura T, Sombuntham T, Sriwongpanich N, Kotchabhakdi N. Prevalence and clinical characteristics of fragile X syndrome at child development clinic, Ramathibodi Hospital. J Med Assoc Thai. 2000;83(1):69-76.
  36. Limprasert P, Ruangdaraganon N, Sura T, Vasiknanonte P, Jinorose U. Molecular screening For fragile X syndrome in Thailand. Southeast Asian J Trop Med Public Health. 1999;30 Suppl 2:114-8.
  37. Manitchotpisit B, Kunachak S, Kulapraditharom B, Sura T. Combined use of fine needle aspiration cytology and polymerase chain reaction in the diagnosis of cervical tuberculouslymphadenitis. J Med Assoc Thai. 1999;82(4):363-8.
  38. Suwanjutha S, Huang NN, Wattanasirichaigoon D, Sura T, Harris A, Macek M Jr. Case report of a Thai male cystic fibrosis patinet with the 1898+ 1G-->T splicing mutation in the CFTR gene: a review of East Asian cases. Mutations in brief no. 196. Online.Hum Mutat. 1998;12(5):361.
  39. Pramoolsinsap C, Poovorawan Y, Sura T, Theamboonlers A, Busagorn N, Kurathong S. Hepatitis G infection and therapeutic response to interferon in HCV-related chronic liver disease. Southeast Asian J Trop Med Public Health. 1998;29(3):480-90.
  40. 2. Ngo EO, Nutter LM, Sura T, Gutierrez PL. Induction of p53 by the concerted actions of aziridine and quinone moieties of diaziquone. Chem Res Toxicol.1998;11(4):360-8.
  41. Sura T, Smith MD, Cowan GM, Walsh AL, White NJ, Krishna S. Polymerase chain reaction For the detection of Burkholderia pseudomallei. Diagn Microbiol Infect Dis. 1997;29(3):121-7.
  42. Sura T, Suwanaluk V, Charoenpan P, Praharktam R, Kiatboonsri C. Clinical use of polymerase chain reaction (PCR) for the diagnosis of sputum smear-negative pulmonary tuberculosis. Journal of Ramathibodi Medical.1997;20(3):231-36.
  43. Sura T, Yamwonge S, Thaisetthawatkul P. Familial Hypercholesterolemiawith mutation of the low density lipoprotein (LDL) receptor gene in a Thai family. Ramathibodi Med J 1996;19(4):200-207.
  44. Boonyakarnjanakom R, Sura T, Phuapradit P, Krishna S. HLA antigens and multiple sclerosis in Thai patients. Rama Med J.1995;18:47-52.
  45. Chaimanowong W, Charoenpan P, Sura T, Charoensub A, Juthangran S. Polymerase Chain Reaction in Treated Pulmonary Tuberculosis. The Thoracic Society of Thailand Newsletter 1995;4(2):8-9.
  46. Sitburana O, Sura T, Phuapradit P, Tulayadechanon S, Likitthanasomb K. Dystrophin gene in a Thai family with Duchennne muscular dystrophy. Rama Med J. 1995;18:96-9.
  47. Sitburana O, Sura T, Visuthiphan P. Diagnosis of Duchenne muscular dystrophy (DMD) by polymerase chain reaction (PCR) in a Thai family. Rama Med J. 1995;18:100-103.
  48. Sura T, Loatharnatas J, Boongird P, Cowan GC. Trinucleotide repeats in Hintington’s disease: a case report Tecratom Pulkes, Ramathaibodi Med Journal.1995;17:4.
  49. Krishna S, Pukrittayakamee S, Supanaranond W, ter Kuile F, Ruprah M, Sura T, White NJ. Fever in uncomplicated Plasmodium falciparum malaria: randomized double-blind Comparison of ibuprofen and paracetamol treatment. Trans R Soc Trop Med Hyg. 1995;89(5):507-9.
  50. Sumethkul V, Jirasiritham S, Sura T, Chiewsilp P. Renal transplantation between identical twins: the application of reciprocal full-thickness skin grafts as a guideline for antirejection therapy. Transplant Proc. 1994;26(4):2141-2. No abstract available.
  51. Hall GW, Franklin IM, Sura T, Thein SL. A novel mutation (nonsense beta 127) in exon 3 of The beta globin gene produces a variable thalassaemic phenotype. Br J Haematol. 1991;79(2):342-4. No abstract available.
  52. Harding AE, Sura T, Tippett P, Boughey AM, Patten JP. Discordance for late-onset Degenerative ataxia in monozygous triplets. J Neurol.1991;238(4):242-3. No abstract available.
  53. Olds RJ, Sura T, Jackson B, Wonke B, Hoffbrand AV, Thein SL. A novel delta 0 mutation in ciswith Hb Knossos: a study of different genetic interactions in three Egyptian families.Br J Haematol. 1991;78(3):430-6.